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rs11110385

From SNPedia

Orientationplus
Stabilizedplus
Make rs11110385(C;C)
Make rs11110385(C;T)
Make rs11110385(T;T)
ReferenceGRCh38 38.1/141
Chromosome12
Position100458927
is asnp
is mentioned by
dbSNPrs11110385
dbSNP (classic)rs11110385
ClinGenrs11110385
ebirs11110385
HLIrs11110385
Exacrs11110385
Gnomadrs11110385
Varsomers11110385
LitVarrs11110385
Maprs11110385
PheGenIrs11110385
Biobankrs11110385
1000 genomesrs11110385
hgdprs11110385
ensemblrs11110385
geneviewrs11110385
scholarrs11110385
googlers11110385
pharmgkbrs11110385
gwascentralrs11110385
openSNPrs11110385
23andMers11110385
SNPshotrs11110385
SNPdbers11110385
MSV3drs11110385
GWAS Ctlgrs11110385
Max Magnitude0
? (C;C) (C;T) (T;T) 28


[PMID 25242139] Association of FXR gene variants with cholelithiasis